A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv543e59



Internal ID20127292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:664352..665150hg38UCSC Ensembl
chr11:664352..665150hg19UCSC Ensembl
chr11:654352..655150hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38799
hg19799
hg18799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3432649, esv3363507
SamplesNA19239, NA12878
Known GenesDEAF1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv543e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer